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HRID 1886498作成日:2026年10月27日

Toluene → Methyl 4-(4-phenoxyphenoxy)benzoate

https://huagongshe.com/reaction/1886498

反応式

関与物質

役割名称HCID仕込み量
反応物TolueneHCID 1140—
反応物Methyl 4-nitrobenzoateHCID 12083—
反応物2-Hydroxydiphenyl etherHCID 75491—
反応物Potassium tert-butoxideHCID 23665647—
溶媒DimethylformamideHCID 6228—
生成物Methyl 4-(4-phenoxyphenoxy)benzoateHCID 19876201—

反応手順

Methyl 4-(4-phenoxyphenoxy)benzoate is synthesized as follows. A mixture of 15.00 g (80.6 mmoles) of -phenoxyphenol, 130 ml of N,N-dimethylformamide and 75 ml of toluene is agitated under nitrogen atmosphere. Potassium t-butoxide (9.32 g, 80.6 mmoles) is added with vigorous stirring and the mixture is heated to reflux. An azeotrope of t-butanol and toluene (85 ml) is collected at temperatures of 120° C. to 135° C. and is discarded. The mixture is cooled to ambient temperature, and a solution of 14.59 g (80.6 mmoles) of methyl 4-nitrobenzoate in 30 ml of N,N-dimethylformamide is added over a period of 15 minutes with cooling in a water bath. The mixture is heated at 100° C. for 14 hours, cooled to 20° C., and quenched with 1500 ml of ice water. The precipitate is filtered, dried in air and dissolved in 500 ml of acetone. The solution is filtered to remove insolubles, and the filtrate is concentrated by evaporation and cooled to precipitate methyl 4-(4-phenoxyphenoxy)benzoate. The recovered product weighs 1 23 g (82 percent yield) and has a melting point of 14° C. as determined by DSC.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05151489
出典データセットuspto-grants-1992_09
ORD IDord-d56031083c1b4238a71fbafe1cac51d7
出典メモuspto-grants-1992_09